Canonical Allele Identifier: PA2826414811
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332901
ClinVar RCV Id: RCV000291685 RCV000304696 RCV000344234 RCV000390621 RCV000470820 RCV000396317 RCV000727772 RCV003317195
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ala9456Thr
CA1999409
NM_001256850.1:c.28366G>A